Intercalated bleach compositions, related methods of manufacture and use

ABSTRACT

The invention relates to compositions, methods of use, and methods of manufacture for an intercalated bleach compound and compositions thereof. The intercalated bleach compound has the formula M x (OCl) y (O) m (OH) n  where M is an alkaline earth metal such as magnesium, calcium or mixture thereof. The values of x and y independently equal any number greater than or equal to 1 (e.g., 1, 2, 3, 4, etc.), and m and n independently equal any number greater than or equal to 0 (e.g., 0, 1, 2, 3, 4, etc.), but m and n are not both 0. In addition, the molar ratio of the alkaline earth metal (e.g., magnesium or calcium) to hypochlorite is at least 3:1. In other words, x is ≧3y. The compounds exhibit excellent stability, little or no chlorine bleach odor, exhibit excellent pH buffering characteristics, and less reactivity with organic materials as compared to alternative chlorine bleach products.

CROSS-REFERENCE TO RELATED APPLICATIONS

The present application is a continuation of U.S. patent applicationSer. No. 14/050,085, filed on Oct. 9, 2013, now U.S. Pat. No. 9,074,164,the disclosure of each of the above applications is incorporated byreference in its entirety.

BACKGROUND OF THE INVENTION

1. The Field of the Invention

The present invention relates to bleaching compounds and bleachingcompositions including such compounds. In addition to such compounds andcompositions, the invention relates to methods of making and using suchcompounds and compositions.

2. Description of Related Art

Sodium hypochlorite is a highly effective cleaning, bleaching andsanitizing agent that is widely used in cleaning and sanitizing varioushard and soft surfaces, in laundry care, etc. Various other chlorinebleach products are available, such as other hypochlorites (e.g.,calcium hypochlorite, lithium hypochlorite, sodium hypochloritephosphate adduct, etc.), isocyanuric acids, isocyanuric acid salts,hydantoins (e.g., dichlorohydantoins), chloroamines (e.g.,trichloromelamine), and others. Such various chlorine bleach productsexhibit various advantages and disadvantages with respect to formulationflexibility, odor (i.e., existing chlorine bleaches exhibit varyingdegrees of the distinctive “bleach” odor), clarity of solutionsformulated with a given bleach product, stability, levels of availablechlorine, chlorine yield, moisture sensitivity, and other criteria.

Generally, any given existing bleach product exhibits a mix of goodcharacteristics with respect to some criteria, and poor characteristicswith respect to other criteria. For example, a sodium hypochloritephosphate adduct bleach product provides excellent solution clarity, andrelatively good characteristics relative to formula flexibility, odor,and moisture sensitivity; however it is undesirable for many purposessuch as laundry detergents because it contains phosphates. While otherbleach products exhibit better characteristics with respect to one ormore of stability, chlorine availability, formula flexibility, etc.;these products often exhibit poor characteristics with respect to othercriteria. In other words, no existing bleach product provides excellentcriteria across a wide range of criteria. As such, there exists acontinuing need for improved chlorine bleach compositions.

BRIEF SUMMARY OF THE INVENTION

One aspect of the present invention is directed to a method of using ableach composition to treat a surface or material. The method includesproviding a bleach composition comprising a bleach compound having theformula M_(x)(OCl)_(y)(O)_(m)(OH)_(n) where M is an alkaline earth metalsuch as magnesium or calcium. The values of x and y may independently beany number greater than or equal to 1 (e.g., 1, 2, 3, 4, etc.), and mand n may independently be any number greater than or equal to 0 (e.g.,0, 1, 2, 3, 4, etc.), but m and n are not both 0. In addition, the molarratio of the alkaline earth metal (e.g., magnesium or calcium) tohypochlorite is at least 3:1. In other words, x is ≧3y. The methodfurther comprises contacting the bleach composition with a surface ormaterial to treat the surface (e.g., hard or soft) or material (e.g.,water, etc.).

Another aspect of the present invention is directed to a method of usinga bleach composition to treat a surface or material. The method includesproviding a bleach composition comprising a bleach compound having theformula Mg_(x)(OCl)_(y)(O)_(m)(OH)_(n). The values of x and y mayindependently be any number greater than or equal to 1 (e.g., 1, 2, 3,4, etc.), and m and n may independently be any number greater than orequal to 0 (e.g., 0, 1, 2, 3, 4, etc.), but m and n are not both 0. Inaddition, the molar ratio of the magnesium to hypochlorite is at least3:1. In other words, x is ≧3y. The method further comprises contactingthe bleach composition with a surface or material to treat the surfaceor material.

Another aspect of the present invention is directed to a method of usinga bleach composition to treat a surface or material. The method includesproviding a bleach composition comprising a surfactant and a bleachcompound having the formula Mg_(x)(OCl)_(y)(O)_(m)(OH)_(n). The valuesof x and y may independently be any number greater than or equal to 1(e.g., 1, 2, 3, 4, etc.), and m and n may independently be any numbergreater than or equal to 0 (e.g., 0, 1, 2, 3, 4, etc.), but m and n arenot both 0. In addition, the molar ratio of the magnesium tohypochlorite is at least 3:1. In other words, x is ≧3y. The methodfurther comprises contacting the bleach composition with a surface ormaterial to treat the surface or material.

Further features and advantages of the present invention will becomeapparent to those of ordinary skill in the art in view of the detaileddescription of preferred embodiments below.

BRIEF DESCRIPTION OF THE DRAWINGS

To further clarify the above and other advantages and features of thepresent invention, a more particular description of the invention willbe rendered by reference to specific embodiments thereof which areillustrated in the drawings located in the specification. It isappreciated that these drawings depict only typical embodiments of theinvention and are therefore not to be considered limiting of its scope.The invention will be described and explained with additionalspecificity and detail through the use of the accompanying drawings inwhich:

FIG. 1 plots percentage available chlorine and percentage yield data forvarious magnesium intercalated bleach compositions according to thepresent invention.

FIG. 2A plots X-ray diffraction (“XRD”) spectroscopy data for anexemplary magnesium intercalated bleach composition.

FIG. 2B plots comparative XRD spectroscopy data for a dibasic magnesiumhypochlorite bleach composition.

FIG. 3A is a bar chart showing comparative stability in a humid storageenvironment after 2 months for magnesium intercalated bleach accordingto the present invention as compared to dibasic magnesium hypochloriteor a mixture of calcium hypochlorite with magnesium oxide.

FIG. 3B is a bar chart showing comparative stability in a humid storageenvironment after 4.5 months for two magnesium intercalated bleachcompositions according to the present invention as compared to a mixtureof calcium hypochlorite with magnesium oxide.

FIG. 4A plots the pH profile of a magnesium intercalated bleachcomposition with 7.7% available chlorine as HCl is added over time.

FIG. 4B plots the concentration of hypochlorite ion within the solutionof FIG. 4A as a function of millimoles of HCl added.

FIG. 5A plots the pH profile of a dibasic magnesium hydroxide bleachcomposition with 34% available chlorine as HCl is added over time.

FIG. 5B plots the concentration of hypochlorite ion within the solutionof FIG. 5A as a function of millimoles of HCl added.

FIG. 6A plots thermodynamic stability data for various MIB compositionsformulated with alcohol ethoxylates.

FIG. 6B plots thermodynamic stability data for various comparativesodium dichloroisocyanurate compositions formulated with alcoholethoxylates.

FIG. 7A plots decomposition thermodynamic stability data for anexemplary MIB composition.

FIG. 7B plots comparative decomposition thermodynamic stability data forcalcium hypochlorite.

FIG. 7C plots comparative decomposition thermodynamic stability data forsodium dichloroisocyanurate.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

I. Definitions

Before describing the present invention in detail, it is to beunderstood that this invention is not limited to particularlyexemplified systems or process parameters that may, of course, vary. Itis also to be understood that the terminology used herein is for thepurpose of describing particular embodiments of the invention only, andis not intended to limit the scope of the invention in any manner.

All publications, patents and patent applications cited herein, whethersupra or infra, are hereby incorporated by reference in their entiretyto the same extent as if each individual publication, patent or patentapplication was specifically and individually indicated to beincorporated by reference.

The term “comprising” which is synonymous with “including,”“containing,” or “characterized by,” is inclusive or open-ended and doesnot exclude additional, unrecited elements or method steps.

The term “consisting essentially of” limits the scope of a claim to thespecified materials or steps “and those that do not materially affectthe basic and novel characteristic(s)” of the claimed invention.

The term “consisting of” as used herein, excludes any element, step, oringredient not specified in the claim.

It must be noted that, as used in this specification and the appendedclaims, the singular forms “a,” “an” and “the” include plural referentsunless the content clearly dictates otherwise. Thus, for example,reference to a “surfactant” includes one, two or more such surfactants.

The term water-soluble polymer as used herein means a polymer whichgives an optically clear solution free of precipitates at aconcentration of 0.001 grams per 100 grams of water, preferably 0.01grams/100 grams of water, more preferably 0.1 grams/100 grams of water,and even more preferably 1 gram or more per 100 grams of water, at 25°C.

As used herein, the term “sanitize” shall mean the reduction ofcontaminants in the inanimate environment to levels considered safeaccording to public health ordinance, or that reduces the bacterialpopulation by significant numbers where public health requirements havenot been established. An at least 99% reduction in bacterial populationwithin a 24 hour time period is deemed “significant.” The term“disinfect” may generally refer to the elimination of many or allpathogenic microorganisms on surfaces with the exception of bacterialendospores. The term “sterilize” may refer to the complete eliminationor destruction of all forms of microbial life and which is authorizedunder the applicable regulatory laws to make legal claims as a“sterilant” or to have sterilizing properties or qualities.

The term “cleaning composition” as used herein, is meant to mean andinclude a cleaning formulation having at least one surfactant.

The term “laundry composition” as used herein, is meant to mean andinclude a laundry formulation having at least one surfactant.

The term “surfactant” as used herein, is meant to mean and include asubstance or compound that reduces surface tension when dissolved inwater or water solutions, or that reduces interfacial tension betweentwo liquids, or between a liquid and a solid. The term “surfactant” thusincludes anionic, nonionic, cationic, zwitterionic and/or amphotericagents.

In the application, effective amounts are generally those amounts listedas the ranges or levels of ingredients in the descriptions, which followhereto. Unless otherwise stated, amounts listed in percentage (“wt %'s”)are in weight percent (based on 100 weight % active) of the particularmaterial present in the referenced composition, any remaining percentagebeing water or an aqueous carrier sufficient to account for 100% of thecomposition, or for solid forms any remaining percentage being magnesiumor calcium salts unless otherwise noted. For very low weightpercentages, the term “ppm” corresponding to parts per million on aweight/weight basis may be used, noting that 1.0 wt % corresponds to10,000 ppm.

Unless defined otherwise, all technical and scientific terms used hereinhave the same meaning as commonly understood by one of ordinary skill inthe art to which the invention pertains. Although a number of methodsand materials similar or equivalent to those described herein can beused in the practice of the present invention, the preferred materialsand methods are described herein.

II. Intercalated Bleach Compositions

The present invention is directed to bleaching compounds andcompositions including such bleaching compounds. The bleaching compoundsare believed to be intercalated bleach compounds that may include analkaline earth hypochlorite species intercalated with oxide and/orhydroxide species. The inventors have found that the intercalated bleachcompounds exhibit excellent stability (e.g., equal to or better than anyother known chlorine bleach species), little or no characteristicchlorine bleach odor as compared to other forms of chlorine bleach,exhibit excellent pH buffering characteristics at significantly gentlerpH ranges (e.g., about 8 to about 11.5) than existing liquid bleachcompositions (11.5 to 13.5). The intercalated bleach compound is stable,even in high humidity environments, and shows relatively less reactivitywith organic materials as compared to other solid chlorine bleachalternatives. The material does not appear to show evidence of anyself-propagating decomposition reactions, can be provided in solid form(which can be dissolved or suspended into aqueous solution), and doesnot readily clump or cake as do many existing alternative chlorinebleaches. The material exhibits better flexibility as to itscompatibility with various adjuvants than existing alternatives, can beformulated to control release of hypochlorite over a desired period oftime, and may be formulated within compositions that are phosphate freewhile providing the above benefits.

As used herein, when referring to the inventive compositions, it ismeant a composition including the intercalated bleach compound. Thecomposition may optionally include further components, if desired.

The compositions may be employed in a very wide range of environmentsand uses, such as laundry detergents or additives (e.g., cleaning andsanitizing laundry), hard and soft surface cleaning, disinfecting andsanitizing, dishwashing, toilet bowl cleaning, disinfecting, andsanitizing, water purification, sanitizers, lotions, and soaps for skindisinfection and care (e.g., hand sanitizer), spot cleaning, stainpre-treatments, additives for building materials (e.g., grout, drywall,paint, etc.) for mold and mildew inhibition purposes, etc.

The composition could be applied directly as a solid or scouringhypochlorite-releasing bleach formulation, such as a toilet bowlsanitizer, dry laundry detergent or additive, or hard surface (e.g.,floors, walls, countertops, etc.) cleaner. The compositions may also beprovided in concentrated water-dilutable forms, such as powders,tablets, or in pouches.

Specific possible uses include, but are not limited to, general cleaning(e.g., hard or soft surface cleaning/disinfection), a solid employed asan odor absorber/destroyer/deodorizer, an additive for animal litter forodor control and antimicrobial benefits, a solid bleach/solid acidmixture that dissolves immediately in water to form a hard surfacedisinfectant, automatic toilet bowl cleaner, bleaching laundry (e.g.,unit dose, a suspension—stable in bottle with additives, which dissolvesin lower pH, dilution by wash water, or a solid powder), a moldinhibitor/allergen prevention and destroyer, liquid solution deliveredby trigger spray or attenuated dual chamber spray bottle, as an aerosolwith an attenuated dual chamber bottle (this is the first possibility ofhaving an aerosol with bleach), skin care/disinfection, buildingmaterials (e.g., grout, paint, drywall, etc.), or any application wherea solid hypochlorite is desired, but the bleach odor typicallyassociated therewith is not.

Because the intercalated bleach compounds can exhibit little to nochlorine bleach odor, they may be used in formulations where this odoris unwanted, while still delivering the cleaning and micro-efficacybenefits associated with liquid hypochlorite solutions.

The compositions may be used indirectly in bleach-generating systems.For example, a solution may be reconstituted from the solid (e.g.,powder) either directly, or by means of a flow through system whereliquid (e.g., water) is passed over or in contact with the solid. Theresulting solution may optionally be filtered.

Hypochlorite release from the intercalated bleach containingcompositions can be controlled through formulation with acids or othercompounds that may aid in the solubility of magnesium and/or calciumsalts. For example, without such additives, a magnesium intercalatedbleach compound may be relatively insoluble, releasing ppm levels ofhypochlorite slowly and approximately linearly over time. With theinclusion of selected additives (e.g., a solid acid), hypochloriterelease can be made to be substantially instantaneous, upon contact withwater. In addition, intercalated bleach compositions in solid formincluding the solid intercalated bleach and a solid acid (e.g.,potassium bisulfate, boric acid, succinic acid, etc.) exhibit excellentstability, without initiation of any acid/base reaction prior tocontacting the solid with water.

The intercalated bleach compounds can be formulated with a wide varietyof adjuvants. For example, the compositions may include a wide range ofsurfactants, acids, chelating agents, fragrances, alcohols, polymers,etc. that are beneficial in cleaning formulations, even where suchadjuvants are organic, including various organic functional groups. Inother words, the intercalated bleach compounds are significantly lessreactive with organic compounds than other hypochlorite bleachalternatives.

The compositions may be adhered to a cleaning wipe substrate to make adry hypochlorite-releasing wipe. In the case of magnesium intercalatedbleach, the magnesium oxide will likely still have some positive chargecharacter, enhancing cleaning performance, allergen cleaning, andmicro-efficacy of the wipe where negatively charged species may bepresent. Such embodiments would also be expected to exhibit increasedstability as compared to current bleach wipe products, due to thestability characteristics of the intercalated bleach compounds ascompared to existing alternatives.

The composition may be in solid form, e.g., in the form of a powder,tablet, or granule. These forms may be used in any application where asolid hypochlorite-releasing bleach is desired. Aqueous or other liquidsolutions may be prepared therefrom.

Methods of using the composition are also disclosed herein. Methods ofusing the composition generally include contacting the composition witha surface (e.g., countertop, floor, laundry) or material (e.g., toiletbowl water) such that the composition treats (e.g., cleans, sanitizesand/or disinfects) the surface or material.

Methods of making the intercalated bleach compounds and compositions arealso disclosed herein. The intercalated bleach compositions aregenerally the product of reaction of an aqueous solution of alkalineearth metal (e.g., calcium) or alkali metal (e.g., sodium) hypochloritesolution mixed with an alkaline earth metal (e.g., magnesium or calcium)salt such as magnesium oxide. For example, a magnesium intercalatedbleach compound may be obtained from the product of evaporation of anaqueous solution of calcium or sodium hypochlorite solution mixed withmagnesium oxide. The intercalated bleach compound has a molar ratio ofalkaline earth metal (e.g., magnesium or calcium) to hypochlorite thatis greater than or equal to 3. A calcium intercalated bleach compoundcould be similarly formed by mixing the hypochlorite solution withcalcium oxide, rather than magnesium oxide.

In an embodiment, the available chlorine concentration may be from about0.01% to about 25%, or from about 0.1% to about 25% %, or from about 1%to about 25%, or from about 2.5% to 25%.

The intercalated bleach compound is believed to generally have theformula M_(x)(OCl)_(y)(O)_(m)(OH)_(n):

wherein M is an alkaline earth metal or mixture of alkaline earthmetals, such as magnesium or calcium or mixtures thereof;

wherein x and y independently equal any number greater than or equal to1 (e.g., 1, 2, 3, 4, etc.);

wherein m and n independently equal 0 or any number greater than 0(e.g., 0, 1, 2, 3, 4, etc.), but m and n are not both 0; and wherein xis ≧3y.

The values of x, y, m, and n may be integers (i.e., whole numbers). Byway of further example, in an embodiment, 2m+n≧5y. In anotherembodiment, x=0.5y+m+0.5n.

One or more adjuvants may be included in the composition. For example,such adjuvants may include, but are not limited to surfactants, acids,builders, water-soluble polymers, and cross-linked water-swellablepolymers.

A. Builders

The composition can contain a builder. In an embodiment, the builder maybe present in an amount ranging from about 1% to about 90%, about 50% toabout 80%, about 10% to about 60%, or about 25% to about 50%. Thebuilder can be selected from inorganic builders (e.g., sulfates,carbonates, bicarbonates, sesquicarbonates, clays, zeolites, silicates,aluminas, aluminasilicates, and mixtures thereof), such as alkali metalcarbonate, alkali metal bicarbonate, alkali metal hydroxide, alkalimetal silicate, alkali metal halide and combinations thereof.

A builder may increase the effectiveness of an included surfactant, canfunction as a softener, a sequestering or chelating agent, a bufferingagent, a diluent or filler, a carrier or a pH adjusting agent in thecomposition. A variety of builders or buffers can be used and theyinclude, but are not limited to, phosphate-silicate compounds, zeolites,alkali metal, ammonium and substituted ammonium polyacetates, trialkalisalts of nitrilotriacetic acid, carboxylates, polycarboxylates,carbonates, bicarbonates, polyphosphates, aminopolycarboxylates,polyhydroxy-sulfonates, sucrose starch derivatives, cellulose gum,bitumen, clay, corn starch, cellulose gum, FeAl aluminide intermetallic,Fuller's earth, lignosulfonate, hydrated lime, molasses, finely groundwaste paper, water, wax, polyacrylic acid and polyacrylates, otherpolymers (polyethyleneimine and polyacrylamide), liquid polybutadineemulsion, adhesives, tar, pitch and mixtures thereof.

Builders, when used, include, but are not limited to, organic acids,mineral acids, alkali metal and alkaline earth salts of silicate,metasilicate, polysilicate, aluminosilicate, borate, borax, sulfates,hydroxide, carbonate, bicarbonate, sesquicarbonate, carbamate,phosphate, polyphosphate, pyrophosphates, triphosphates,tetraphosphates, ammonia, hydroxide, monoethanolamine,monopropanolamine, diethanolamine, dipropanol-amine, triethanolamine,and 2-amino-2methylpropanol. Other suitable buffers include ammoniumcarbamate, citric acid, formic acid, formate salts and acetic acid.

Additional details of builders and buffers can be found in WO 95/07971,which is incorporated herein by reference. The term silicate is meant toencompass silicate, metasilicate, polysilicate, aluminosilicate andsimilar compounds. More specific examples include sodium tetraborate,sodium carbonate, sodium bicarbonate, sodium sesquicarbonate, potassiumcarbonate, potassium bicarbonate, sodium and potassium zeolites.Exemplary organic non-phosphate builders and sequestrant salts includealkali metal salts of polycarboxylic acids and nitriloacetic acid. Morespecific examples include monosodium, disodium and trisodium citrate,and tetrasodium ethylenediaminetetraacetate (EDTA-Na₄), diethylenetriamine pentaacetic acid (DTPA), dipropylethyl tetraamine, ethylenediamine disuccinic salt, ethylenediamine (EDA) and derivatives,diethylenetriamine (DETA), aminoethylethanolamine (AEEA). Salts andderivatives of organic acids (e.g., citric acid and tartaric acid,glutamic acid, formic acid, succinic acid), and amino acid basedcomponents may also be suitable for use.

B. Polymers

The composition can contain a water-soluble polymer. Examples ofwater-soluble polymer include, but are not limited to, polycarboxylate,sulfonated carboxylate, polysulfonate, polyvinylpyrrolidone (“PVP”),polyacrylic acid, polyacrylate, copolymers and mixtures thereof, andmixtures thereof.

Examples of polycarboxylate include, but are not limited to, polymerswith sufficient carboxylate ions to achieve water solubility.Carboxylate ions may be derived from various monomers including acrylicacid, maleic acid and maleic anhydride. Copolymers of differentcarboxylate-containing monomers are also suitable as well as copolymerswith non-carboxylate containing monomers such as methacrylate,acrylonitrile, styrene, ethylene, propylene, and many others. Mixturesof carboxylate containing polymers can also be used.

In an embodiment, the molecular weight of the water-soluble polymer maybe between about 1,000 to about 100,000 Daltons, about 2,000 to about80,000 Daltons, about 3,000 to about 10,000 Daltons, or about 3,000 toabout 5,000 Daltons. The water-soluble polymer may be present in anamount ranging from about 0.1% to about 60%, about 5% to about 50%,about 10% to about 40%, or about 20% to about 30%.

The composition may contain a cross-linked water-swellable polymer.Examples of water-swellable polymer include, but are not limited to,cross-linked polycarboxylate, cross-linked polysulfonate, cross-linkedcarboxymethylcellulose, cross-linked PVP, cellulose, sodiumcarboxymethylcellulose and mixtures thereof.

In an embodiment, the molecular weight of the water-swellable polymermay be between about 1,000 to about 100,000 Daltons, about 2,000 toabout 80,000 Daltons, or about 3,000 to about 10,000 Daltons or about3,000 Daltons to about 5,000 Daltons. The water-swellable polymer may bepresent in an amount ranging from about 0.1% to about 60%, about 5% toabout 50%, about 10% to about 40%, or about 20% to about 30%.

Polymers may also include both high and low molecular weight polymersand any monomers or oligomers, waxes, polymeric surfactants, latex,silicones, silicone polyether, copolymers, maleic/acrylic copolymers,dimethicone, hydrogenated castor oil, saccharides, and any weightpolyethylene glycol. In addition, the category of polymers could includebut is not limited to polyethyleneimine ethoxylate propoxylate,diquaternium ethoxysulfate, polyethyleneimine ethoxylate, glycerine,PEG-136 polyvinylacetate, polyacrylamide quaternium chloride.

C. Acids

The composition may contain an acid. Inclusion of an acid (e.g., a solidacid) may aid in controlling the release profile of hypochlorite fromthe intercalated bleach compound. Examples of acids that can be usedwith the present invention may include, but are not limited to, sulfonicacid, sulfamic acid, boric acid, siliceous acids, hydrochloric acid,sulfuric acid, phosphoric acid, dicarboxylic acid, monocarboxylic acid,aminocarboxylic acid, 2-hydroxy-1,2,3-propanetricarboxylic acid, organicacids such as but not limited to citric acid, adipic acid, succinicacid, acrylic acid, polyacrylic acid, lauric acid, lactic acid, aceticacid, hydroxyacetic acid, acid salts, and mixtures thereof. Specificexamples of acids, include but are not limited to, succinic acid,glutaric acid, 3-pyridine sulfonic acid, dodecyl benzene sulfonic acid,and mixtures thereof. In an embodiment, an included acid may be in solidform. Examples of such solid acids include inorganic acidic salts suchas potassium bisulfate, magnesium chloride or other acidic metal salts,hydrogen phosphate salts, sodium bicarbonate, organic acids such assuccinic acid, fatty acids, nucleic acids palmitic acid, and Lewis acidssuch as boric acid. Acidic gases or nonmetal oxides may also beincluded, for example carbon dioxide. Any acids may be present in anamount ranging from about 0.1% to about 75%, about 5% to about 50%,about 10% to about 40%, or about 20% to about 30%.

D. Bases

The composition may contain one or more bases selected from inorganic,organic, and amphoteric bases and mixtures thereof. Inclusion of a base(e.g., a solid base) may aid in controlling the release profile ofhypochlorite from the intercalated bleach compound. Examples of basesthat can be used with the present invention may include, but are notlimited to, any hydroxide salt, metal oxides, amphoteric oxides,carbonates, phosphates, borate, citrate, acetate, formate and anymixtures or salts thereof. Any bases may be present in an amount rangingfrom about 0.1% to about 75%, about 5% to about 50%, about 10% to about40%, or about 20% to about 30%.

E. Surfactants

The composition may contain one or more surfactants selected fromnonionic, anionic, cationic, ampholytic, amphoteric and zwitterionicsurfactants and mixtures thereof. A typical listing of anionic,ampholytic, and zwitterionic classes, and species of these surfactants,is given in U.S. Pat. No. 3,929,678 to Laughlin and Heuring. A list ofsuitable cationic surfactants is given in U.S. Pat. No. 4,259,217 toMurphy. The surfactants may be present at a level of from about 0.1% toabout 75%, from about 5% to about 50%, or from about 10% to about 30%.

The composition may comprise an anionic surfactant. Exemplary anionicsurfactants may include salts (including, for example, sodium,potassium, ammonium, and substituted ammonium salts such as mono-, di-and tri-ethanolamine salts) of the anionic sulfate, sulfonate,carboxylate and sarcosinate surfactants. Anionic surfactants maycomprise a sulfonate or a sulfate surfactant. Anionic surfactants maycomprise an alkyl sulfate, a linear or branched alkyl benzene sulfonate,or an alkyldiphenyloxide disulfonate, alkyl disulfates, alcoholsulfates, sodium palmitate, or as salts of fatty acids as describedherein.

Other anionic surfactants include the isethionates such as the acylisethionates, N-acyl taurates, fatty acid amides of methyl tauride,alkyl succinates and sulfosuccinates, monoesters of sulfosuccinate (forinstance, saturated and unsaturated C12-C18 monoesters) diesters ofsulfosuccinate (for instance saturated and unsaturated C6-C14 diesters),N-acyl sarcosinates. Resin acids and hydrogenated resin acids are alsosuitable, such as rosin, hydrogenated rosin, and resin acids andhydrogenated resin acids present in or derived from tallow oil. Anionicsulfate surfactants suitable for use herein include the linear andbranched primary and secondary alkyl sulfates, alkyl ethoxysulfates,fatty oleoyl glycerol sulfates, alkyl phenol ethylene oxide ethersulfates, the C5-C17acyl-N—(C1-C4 alkyl) and —N—(C1-C2 hydroxyalkyl)glucamine sulfates, and sulfates of alkylpolysacchanides such as thesulfates of alkylpolyglucoside (the nonionic nonsulfated compounds beingdescribed herein). Alkyl sulfate surfactants may be selected from thelinear and branched primary C10-C18 alkyl sulfates, the C11-C15 branchedchain alkyl sulfates, or the C12-C14 linear chain alkyl sulfates.

Alkyl ethoxysulfate surfactants may be selected from the groupconsisting of the C10-C18 alkyl sulfates, which have been ethoxylatedwith from 0.5 to 20 moles of ethylene oxide per molecule. The alkylethoxysulfate surfactant may be a C11-C18, or a C11-C15 alkyl sulfatewhich has been ethoxylated with from 0.5 to 7, or from 1 to 5, moles ofethylene oxide per molecule. Mixtures of alkyl sulfate and/or sulfonateand alkyl ethoxysulfate surfactants may be employed. Such mixtures havebeen disclosed in PCT Patent Application No. WO 93/18124.

Anionic sulfonate surfactants suitable for use herein include the saltsof C5-C20 linear alkylbenzene sulfonates, alkyl ester sulfonates, C6-C22primary or secondary alkane sulfonates, C6-C24 olefin sulfonates,sulfonated polycarboxylic acids, alkyl glycerol sulfonates, fatty acylglycerol sulfonates, fatty oleyl glycerol sulfonates, and any mixturesthereof. Suitable anionic carboxylate surfactants include the alkylethoxy carboxylates, the alkyl polyethoxy polycarboxylate surfactantsand the soaps (“alkyl carboxyls”), especially certain secondary soaps asdescribed herein. Suitable alkyl ethoxy carboxylates include those withthe formulaRO(CH₂CH₂O)_(x)CH₂COO⁻M⁺

wherein R is a C6 to C18 alkyl group, x ranges from 0 to 10, and theethoxylate distribution is such that, on a weight basis, the amount ofmaterial where x is 0 is less than 20% and M is a cation. Suitable alkylpolyethoxypolycarboxylate surfactants include those having the formulaRO—(CHR¹—CHR²—O)—R³ wherein R is a C6 to C18 alkyl group, x is from 1 to25, R¹ and R² are selected from the group consisting of hydrogen, methylacid radical, succinic acid radical, hydroxysuccinic acid radical, andmixtures thereof, and R³ is selected from the group consisting ofhydrogen, substituted or unsubstituted hydrocarbon having between 1 and8 carbon atoms, and mixtures thereof.

Suitable soap surfactants include the secondary soap surfactants, whichcontain a carboxyl unit connected to a secondary carbon. Suitablesecondary soap surfactants for use herein are water-soluble membersselected from the group consisting of the water-soluble salts of2-methyl-1-undecanoic acid, 2-ethyl-1-decanoic acid, 2-propyl-1-nonanoicacid, 2-butyl-1-octanoic acid and 2-pentyl-1-heptanoic acid. Certainsoaps may also be included as suds suppressors.

Other suitable anionic surfactants are the alkali metal sarcosinates offormula R—CON(R¹) CH—)COOM, wherein R is a C5-C17 linear or branchedalkyl or alkenyl group, R¹ is a C1-C4 alkyl group and M is an alkalimetal ion. Examples are the myristyl and oleoyl methyl sarcosinates inthe form of their sodium salts.

Other suitable surfactants include fatty acid sarosinates which aremild, biodegradable anionic surfactants derived from fatty acids andsarcosine (amino acid). Sarcosine is the N-methyl derivative of glycine.Sarcosine is a natural amino acid found in muscles and other tissues.Sarcosine is found naturally as an intermediate in the metabolism ofcholine to glycine. In a preferred embodiment, the sarcosines are acylsarcosines. Examples of acyl sarcosines include, but are not limited to,cocoyl sarcosine, lauroyl sarcosine, myristoyl sarcosine, oleoylsarcosine, stearoyl sarcosine which are modified fatty acids. The saltsof acyl sarcosines are referred to acyl sarcosinates. Acyl sarcosinatesuseful herein include, for example, those having a formula:RCON(CH₃)CH2COOX

wherein R is an alkyl or alkenyl having from 8 to 22 carbon atoms,preferably from 12 to 18 carbon atoms, more preferably from 12 to 14carbon atoms; and X is a sodium, potassium, ammonium, ortriethanolamine.

Examples of acyl sarcosinates that can be used with the presentinvention include, but not limited to, sodium coccyl sarcosinate, sodiumlauroyl sarcosinate and sodium myristoyl sarcosinate, sodium oleoylsarcosinate, sodium stearoyl sarcosinate, ammonium coccyl sarcosinate,ammonium lauroyl sarcosinate and ammonium myristoyl sarcosinate,ammounium oleoyl sarcosinate and ammonium stearoyl sarcosinate.Commercially available preferred acyl sarcosinates include, but are notlimited to, for example, sodium lauroyl sarcosinate having the tradenameHamposyl® L30 which is available from Hampshire Chemicals, and sodiumcocoyl sarcosinate having the tradename Hamposyl® C30 which is availablefrom Hampshire Chemicals.

Other suitable surfactants may include fatty alcohol sulfate which has ahigher alcohol or alkyl group is normally in the range of 10 to 18carbon atoms. The cation will almost invariably be sodium or willinclude sodium, although other cations, such as triethanolamine,potassium, ammonium, magnesium and calcium may also be employed.Exemplary fatty alcohol sulfates may include those wherein the fattyalcohol is essentially saturated and is of carbon content(s) within the10 to 18 carbon atoms range, preferably 10 or 12 to 14 or 16 carbonatoms, such as 12 to 16, or that is derived from coconut oil (coco),palm oil, or palm kernel oil. Lauryl sulfates, and particularly, sodiumlauryl sulfate, may be preferred primary detergents but such designationalso may apply to such detergents wherein the carbon chain length of thealcohol is not limited to 12 carbon atoms, but is primarily (over 50%and normally over 70 or 75%) of 12 to 14 carbon atoms. Such materialsmay be obtained from natural sources, such as coconut oil and palmkernel oil. In one embodiment, the fatty alcohol sulfate is a C12-C18fatty alcohol sulfate. In another embodiment, the fatty alcohol sulfateis a C12-C16 fatty alcohol sulfate. In another embodiment, the fattyalcohol sulfate is a C12-C14 fatty alcohol sulfate. In anotherembodiment, the fatty alcohol is a C12 fatty alcohol sulfate. In anotherembodiment, the fatty alcohol sulfate is sodium lauryl sulfate. In aspecific embodiment, the fatty alcohol sulfate is a sodium coco fattyalcohol sulfate.

Suitable amphoteric surfactants for use herein may include the amineoxide surfactants and the alkyl amphocarboxylic acids. Suitable amineoxides include those compounds having the formula R³(OR⁴)_(X)NO(R⁵)₂wherein R³ is selected from an alkyl, hydroxyalkyl, acylamidopropyl andalkylphenyl group, or mixtures thereof, containing from 8 to 26 carbonatoms; R⁴ is an alkylene or hydroxyalkylene group containing from 2 to 3carbon atoms, or mixtures thereof, x is from 0 to 5, preferably from 0to 3; and each R⁵ is an alkyl or hydroxyalkyl group containing from 1 to3, or a polyethylene oxide group containing from 1 to 3 ethylene oxidegroups. Suitable amine oxides are C10-C18 alkyl dimethylamine oxide, andC10-18 acylamido alkyl dimethylamine oxide. A suitable example of analkyl amphodicarboxylic acid is Miranol™ C2M Conc. manufactured byMiranol, Inc., Dayton, N.J.

Zwitterionic surfactants can also be incorporated into the compositions.These surfactants can be broadly described as derivatives of secondaryand tertiary amines, derivatives of heterocyclic secondary and tertiaryamines, or derivatives of quaternary ammonium, quaternary phosphonium ortertiary sulfonium compounds. Betaine and sultaine surfactants may beexemplary zwittenionic surfactants for use herein.

Suitable betaines are those compounds having the formula R(R¹)₂N⁺R²COO⁻wherein R is a C6-C18 hydrocarbyl group, each R¹ is typically C1-C3alkyl, and R² is a C1-C5 hydrocarbyl group. Suitable betaines are C12-18dimethyl-ammonio hexanoate and the C10-18 acylamidopropane (or ethane)dimethyl (or diethyl) betaines. Complex betaine surfactants are alsosuitable for use herein.

Suitable cationic surfactants to be used herein may include thequaternary ammonium surfactants. The quaternary ammonium surfactant maybe a mono C6-C16, or a C6-C10 N-alkyl or alkenyl ammonium surfactantwherein the remaining N positions are substituted by methyl,hydroxyethyl or hydroxypropyl groups. Suitable are also themono-alkoxylated and bis-alkoxylated amine surfactants. Additionalsuitable cationic surfactants include coco fatty acid diethanolamine,hydrogenated palm tea ester quat, and cationic ethyoxylate fatty acids.

Another group of cationic surfactants that may be suitable for use iscationic ester surfactants. The cationic ester surfactant is a compoundhaving surfactant properties comprising at least one ester (i.e. —COO—)linkage and at least one cationically charged group. Suitable cationicester surfactants, including choline ester surfactants, have for examplebeen disclosed in U.S. Pat. Nos. 4,228,042, 4,239,660 and 4,260,529. Theester linkage and cationically charged group may be separated from eachother in the surfactant molecule by a spacer group consisting of a chaincomprising at least three atoms (i.e. of three atoms chain length), orfrom three to eight atoms, or from three to five atoms, or three atoms.The atoms forming the spacer group chain are selected from the groupconsisting, of carbon, nitrogen and oxygen atoms and any mixturesthereof, with the proviso that any nitrogen or oxygen atom in said chainconnects only with carbon atoms in the chain. Thus spacer groups having,for example, —O—O— (i.e. peroxide), —N—N—, and —N—O— linkages areexcluded, whilst spacer groups having, for example —CH₂—O—, CH₂— and—CH₂—NH—CH₂— linkages are included. The spacer group chain may compriseonly carbon atoms, or the chain is a hydrocarbyl chain.

The composition may comprise cationic mono-alkoxylated aminesurfactants, for instance, of the general formula: R¹R²R³N⁺ApR⁴X⁻wherein R¹ is an alkyl or alkenyl moiety containing from about 6 toabout 18 carbon atoms, or from 6 to about 16 carbon atoms, or from about6 to about 14 carbon atoms; R² and R³ are each independently alkylgroups containing from one to about three carbon atoms, for instance,methyl, for instance, both R² and R³ are methyl groups; R⁴ is selectedfrom hydrogen, methyl and ethyl; X⁻ is an anion such as chloride,bromide, methylsulfate, sulfate, or the like, to provide electricalneutrality; A is a alkoxy group, especially a ethoxy, propoxy or butoxygroup; and p is from 0 to about 30, or from 2 to about 15, or from 2 toabout 8. The ApR⁴ group in the formula may have p=1 and is ahydroxyalkyl group, having no greater than 6 carbon atoms whereby the—OH group is separated from the quaternary ammonium nitrogen atom by nomore than 3 carbon atoms. Suitable ApR⁴ groups are —CH₂CH₂—OH,—CH₂CH₂CH₂—OH, —CH₂CH(CH₃)—OH and —CH(CH₃)CH₂—OH. Suitable R¹ groups arelinear alkyl groups, for instance, linear R¹ groups having from 8 to 14carbon atoms.

Suitable cationic mono-alkoxylated amine surfactants for use herein maybe of the formula R¹(CH₃)(CH₃)N⁺(CH₂CH₂O)₂₋₅H X⁻ wherein R¹ is C10-C18hydrocarbyl and mixtures thereof, especially C10-C14 alkyl, or C10 andC12 alkyl, and X is any convenient anion to provide charge balance, forinstance, chloride or bromide.

As noted, compounds of the foregoing type include those wherein theethoxy (CH₂CH₂O) units (EO) are replaced by butoxy, isopropoxy[CH(CH₃)CH₂O] and [CH₂CH(CH₃)O] units (i-Pr) or n-propoxy units (Pr), ormixtures of EO and/or Pr and/or i-Pr units.

The cationic bis-alkoxylated amine surfactant may have the generalformula: R¹R²N⁺ApR³A′qR⁴X⁻ wherein R¹ is an alkyl or alkenyl moietycontaining from about 8 to about 18 carbon atoms, or from 10 to about 16carbon atoms, or from about 10 to about 14 carbon atoms; R² is an alkylgroup containing from one to three carbon atoms, for instance, methyl;R³ and R⁴ can vary independently and are selected from hydrogen, methyland ethyl, X⁻ is an anion such as chloride, bromide, methylsulfate,sulfate, or the like, sufficient to provide electrical neutrality. A andA′ can vary independently and are each selected from C1-C4 alkoxy, forinstance, ethoxy, (i.e., —CH₂CH₂O—), propoxy, butoxy and mixturesthereof, p is from 1 to about 30, or from 1 to about 4 and q is from 1to about 30, or from 1 to about 4, or both p and q are 1.

Suitable cationic bis-alkoxylated amine surfactants for use herein maybe of the formula R¹CH₃N⁺(CH₂CH₂OH)(CH₂CH₂OH) X⁻, wherein R¹ is C10-C18hydrocarbyl and mixtures thereof, or C10, C12, C14 alkyl and mixturesthereof, X⁻ is any convenient anion to provide charge balance, forexample, chloride. With reference to the general cationicbis-alkoxylated amine structure noted above, since in one examplecompound R¹ is derived from (coconut) C12-C14 alkyl fraction fattyacids, R² is methyl and ApR³ and A′qR⁴ are each monoethoxy.

Other cationic bis-alkoxylated amine surfactants useful herein includecompounds of the formula: R¹R²N⁺—(CH₂CH₂O)_(p)H—(CH₂CH₂O)_(q)H X⁻wherein R¹ is C10-C18 hydrocarbyl, or C10-C14 alkyl, independently p is1 to about 3 and q is 1 to about 3, R² is C1-C3 alkyl, for example,methyl, and X⁻ is an anion, for example, chloride or bromide.

Other compounds of the foregoing type include those wherein the ethoxy(CH₂CH₂O) units (EO) are replaced by butoxy (Bu) isopropoxy[CH(CH₃)CH₂O] and [CH₂CH(CH₃)O] units (i-Pr) or n-propoxy units (Pr), ormixtures of EO and/or Pr and/or i-Pr units.

The inventive compositions may include at least one fluorosurfactantselected from nonionic fluorosurfactants, cationic fluorosurfactants,and mixtures thereof which are soluble or dispersible in the aqueouscompositions being taught herein, sometimes compositions which do notinclude further detersive surfactants, or further organic solvents, orboth. Suitable nonionic fluorosurfactant compounds are found among thematerials presently commercially marketed under the tradename Fluorad®(ex. 3M Corp.) Exemplary fluorosurfactants include those sold asFluorad® FC-740, generally described to be fluorinated alkyl esters;Fluorad® FC-430, generally described to be fluorinated alkyl esters;Fluorad® FC-431, generally described to be fluorinated alkyl esters;and, Fluorad® FC-170-C, which is generally described as beingfluorinated alkyl polyoxyethlene ethanols.

An example of a suitable cationic fluorosurfactant compound may have thefollowing structure: C_(n)F_(2n+1)SO₂NHC₃H₆N⁺(CH₃)₃I⁻ where n˜8. Thiscationic fluorosurfactant is available under the tradename Fluorad®FC-135 from 3M. Another example of a suitable cationic fluorosurfactantis F₃—(CF₂)_(n)—(CH₂)_(m)SCH₂CHOH—CH₂—N⁺R₁R₂R₃Cl⁻wherein: n is 5-9 and m is 2, and R₁, R₂ and R₃ are —CH₃. This cationicfluorosurfactant is available under the tradename ZONYL® FSD (availablefrom DuPont, described as2-hydroxy-3-((gamma-omega-perfluoro-C₆₋₂₀-alkyl)thio)-N,N,N-trimethyl-1-propylammonium chloride). Other cationic fluorosurfactants that may besuitable for use in the present invention are also described in EP866,115 to Leach and Niwata. The fluorosurfactant selected from thegroup of nonionic fluorosurfactant, cationic fluorosurfactant, andmixtures thereof may be present in amounts of from 0.001 to 5% wt.,preferably from 0.01 to 1% wt., and more preferably from 0.01 to 0.5%wt.

The composition may comprise a nonionic surfactant. Essentially anyalkoxylated nonionic surfactants are suitable herein, for instance,ethoxylated and propoxylated nonionic surfactants. Alkoxylatedsurfactants can be selected from the classes of the nonionic condensatesof alkyl phenols, nonionic ethoxylated alcohols, nonionicethoxylated/propoxylated fatty alcohols, nonionic ethoxylate/propoxylatecondensates with propylene glycol, and the nonionic ethoxylatecondensation products with propylene oxide/ethylene diamine adducts.

The condensation products of aliphatic alcohols with from 1 to 25 molesof alkylene oxide, particularly ethylene oxide and/or propylene oxide,may be suitable for use herein. The alkyl chain of the aliphatic alcoholcan either be straight or branched, primary or secondary, and generallycontains from 6 to 22 carbon atoms. Also suitable are the condensationproducts of alcohols having an alkyl group containing from 8 to 20carbon atoms with from 2 to 10 moles of ethylene oxide per mole ofalcohol.

Polyhydroxy fatty acid amides suitable for use herein may include thosehaving the structural formula R²CONR¹Z wherein: R¹ is H, C1-C4hydrocarbyl, 2-hydroxyethyl, 2-hydroxypropyl, ethoxy, propoxy, or amixture thereof, for instance, C1-C4 alkyl, or C1 or C2 alkyl; and R² isa C5-C31 hydrocarbyl, for instance, straight-chain C5-C19 alkyl oralkenyl, or straight-chain C9-C17 alkyl or alkenyl, or straight-chainC11-C17 alkyl or alkenyl, or mixture thereof, and Z is apolyhydroxyhydrocarbyl having a linear hydrocarbyl chain with at least 3hydroxyls directly connected to the chain, or an alkoxylated derivative(for example, ethoxylated or propoxylated) thereof. Z may be derivedfrom a reducing sugar in a reductive amination reaction, for example, Zis a glycityl.

Suitable fatty acid amide surfactants may include those having theformula: R¹CON(R²)₂ wherein R¹ is an alkyl group containing from 7 to21, or from 9 to 17 carbon atoms and each R² is selected from the groupconsisting of hydrogen, C1-C4 alkyl, C1-C4 hydroxyalkyl, and—(C₂H₄O)_(x)H, where x is in the range of from 1 to 3.

Alkylpolysaccharides that may be suitable for use herein are disclosedin U.S. Pat. No. 4,565,647 to Llenado, having a hydrophobic groupcontaining from 6 to 30 carbon atoms and a polysaccharide, e.g., apolyglycoside, hydrophilic group containing from 1.3 to 10 saccharideunits. Alkylpolyglycosides may have the formula:R²O(C_(n)H_(2n)O)_(t)(glycosyl)_(x) wherein R² is selected from thegroup consisting of alkyl, alkylphenyl, hydroxyalkyl,hydroxyalkylphenyl, and mixtures thereof in which the alkyl groupscontain from 10 to 18 carbon atoms; n is 2 or 3; t is from 0 to 10, andx is from 1.3 to 8. The glycosyl may be derived from glucose.

Other suitable nonionic surfactants may include food safe nonionicsurfactants. Examples of food safe nonionic surfactants are sucroseesters, such as sucrose cocoate available from Croda, and sorbitanesters, such as polyoxyethylene(20) sorbitan monooleate from J. T. Bakerand polyoxyethylene(20) sorbitan monolaurate from Uniquema. Otherexamples of food safe nonionic surfactants are given in GenerallyRecognized As Safe (GRAS) lists, as described below.

In an embodiment, the compositions may specifically contain alkylpolyglucoside (“APG”) surfactant. Suitable alkyl polyglucosidesurfactants may include alkylpolysaccharides that are disclosed in U.S.Pat. No. 5,776,872 to Giret et al.; U.S. Pat. No. 5,883,059 to Furman etal.; U.S. Pat. No. 5,883,062 to Addison et al.; and U.S. Pat. No.5,906,973 to Ouzounis et al., which are all incorporated by reference.Suitable alkyl polyglucosides for use herein may also be disclosed inU.S. Pat. No. 4,565,647 to Llenado, describing alkylpolyglucosideshaving a hydrophobic group containing from about 6 to about 30 carbonatoms, or from about 10 to about 16 carbon atoms and polysaccharide,e.g., a polyglycoside, hydrophilic group containing from about 1.3 toabout 10, or from about 1.3 to about 3, or from about 1.3 to about 2.7saccharide units. Optionally, there can be a polyalkyleneoxide chainjoining the hydrophobic moiety and the polysaccharide moiety. A suitablealkyleneoxide may be ethylene oxide. Typical hydrophobic groups includealkyl groups, either saturated or unsaturated, branched or unbranchedcontaining from about 8 to about 18, or from about 10 to about 16,carbon atoms. Suitably, the alkyl group can contain up to about 3hydroxy groups and/or the polyalkyleneoxide chain can contain up toabout 10, or less than about 5, alkyleneoxide moieties. Suitable alkylpolysaccharides are octyl, nonyldecyl, undecyldodecyl, tridecyl,tetradecyl, pentadecyl, hexadecyl, heptadecyl, and octadecyl, di-, tri-,tetra-, penta-, and hexaglucosides, galactosides, lactosides, glucoses,fructosides, fructoses and/or galactoses. Suitable mixtures includecoconut alkyl, di-, tri-, tetra-, and pentaglucosides and tallow alkyltetra-, penta-, and hexaglucosides.

Suitable alkylpolyglycosides (or alkylpolyglucosides) have the formula:R²O(C_(n)H_(2n)O)_(t)(glucosyl)_(x) wherein R² is selected from thegroup consisting of alkyl, alkylphenyl, hydroxyalkyl,hydroxyalkylphenyl, and mixtures thereof in which the alkyl groupscontain from about 10 to about 18, preferably from about 12 to about 14,carbon atoms; n is about 2 or about 3, preferably about 2; t is from 0to about 10, preferably 0; and x is from about 1.3 to about 10,preferably from about 1.3 to about 3, most preferably from about 1.3 toabout 2.7. The glycosyl may be derived from glucose. To prepare thesecompounds, the alcohol or alkylpolyethoxy alcohol is formed first andthen reacted with glucose, or a source of glucose, to form the glucoside(attachment at the 1-position). The additional glycosyl units can thenbe attached between their 1-position and the preceding glycosyl units2-, 3-, 4- and/or 6-position, preferably predominantly the 2-position.

A group of alkyl glycoside surfactants suitable for use in the practiceof this invention may be represented by formula I below:RO—(R²O)_(y)-(G)_(x)Z_(b)  (I)wherein R is a monovalent organic radical containing from about 6 toabout 30 (preferably from about 8 to about 18) carbon atoms; R² is adivalent hydrocarbon radical containing from about 2 to about 4 carbonatoms; O is an oxygen atom; y is a number which has an average valuefrom about 0 to about 1 and is preferably 0; G is a moiety derived froma reducing saccharide containing 5 or 6 carbon atoms; and x is a numberhaving an average value from about 1 to 5 (preferably from 1.1 to 2); Zis O₂M¹, O₂CR³, O(CH₂), CO₂M¹, OSO₃M¹, or O(CH₂)SO₃M¹; R³ is (CH₂)CO₂M¹or CH═CHCO₂M¹; (with the proviso that Z can be O₂M¹ only if Z is inplace of a primary hydroxyl group in which the primary hydroxyl-bearingcarbon atom, —CH₂OH, is oxidized to form a —CO₂M¹ group); b is a numberfrom 0 to 3x+1 preferably an average of from 0.5 to 2 per glycosalgroup; p is 1 to 10, M¹ is H⁺ or an organic or inorganic cation, suchas, for example, an alkali metal, ammonium, monoethanolamine, orcalcium. As defined in Formula I, R is generally the residue of a fattyalcohol having from about 8 to 30 or 8 to 18 carbon atoms. Suitablealkylglycosides include, for example, APG 325® (a C₉-C₁₁ alkylpolyglycoside available from Cognis Corporation), APG 625® (a C₁₀-C₁₆alkyl polyglycoside available from Cognis Corporation), Dow Triton®CG110 (a C₈-C₁₀ alkyl polyglyco-side available from Dow ChemicalCompany), AG6202® (a C₈ alkyl polyglycoside available from Akzo Nobel)Glucopon® 425N (a C₈₋C₁₆ alkyl polyglycoside available from CognisCorporation), Glucopon® 215 (a C₈₋C₁₀ alkyl polyglycoside available fromCognis Corporation), Glucpon® 225 (a C₈₋C₁₀ alkyl polyglycosideavailable from Cognis Corporation) and Alkadet 150 (a C₈-C₁₀ alkylpolyglycoside available from Huntsman Corporation). A C8 to C10alkylpoly-glucoside includes alkylpoly-glucosides wherein the alkylgroup is substantially C8 alkyl, substantially C10 alkyl, or a mixtureof substantially C8 and C10 alkyl. Additionally, short chain APGs suchas C4 and/or C6 or mixtures thereof may be suitable with the presentinvention.

E. Additional Adjuvants

Exemplary specific chelating agent sequestrants and/or opticalbrightener components that may be used include, but are not limited to,sodium polyacrylate (e.g., ACCUSOL™ 445N), Na₃ methyl glycine diacetate(e.g., TRILON® M LIQUID), Na₄ glutamic acid diacetate (DISSOLVINE®GL47S), hybrid biopolymers (e.g., ALCOGUARD® HS5240), sodiumpolyitaconate (e.g., ITACONIX™ DSP2K-US), Na_(x) carboxymethyl inulin(COSUN CMI 25-40D or DEQUEST® SPE 15625), TINOSORB FB,triazine-stilbenes including di-, tetra-, or hex-sulfonated derivatives,coumarins, imidazolines, diazoles, triazoles, benzoxazolines,biphenyl-stilbenes and combinations thereof.

Various polyacrylates are of course suitable for use. Examples of suchsequestrants are disclosed in U.S. Pat. Nos. 6,211,131 and 6,297,209,each of which is herein incorporated by reference in its entirety.

The composition may include one or more preservatives. When used, suchadjuvants may include, but are not limited to, methyl, ethyl and propylparabens, phosphates such as trisodium phosphate, short chain organicacids (e.g. acetic, lactic and/or glycolic acids), bisguanidinecompounds (e.g. DANTAGARD and/or GLYDANT) and/or short chain alcohols(e.g. ethanol and/or IPA). Additional details of exemplary preservativesare disclosed in U.S. Publication 2013/0028990, incorporated herein byreference.

Solvents other than water may also be employed (e.g., ethanol,isopropanol, glycol ethers, etc.).

Surfactants, silicates, builders, sequestrants, chelating agents,preservatives, fluorescent whitening agents, optical brighteners,fragrances, dyes, pigments, fillers, diluents, desiccants, buffers,solid processing aids, preservatives, colorants, anti-corrosioninhibitors, fragrances, anti-deposition agents, hydrotropes, polymerdispersants (e.g., alcohol ethoxylates), deflocculants, plasticizers,superplasticizers, emulsifiers, detergents, other disinfectants orantimicrobials (e.g., quaternary ammonium compounds, essential oils,metal salts, silver, zinc, enzymes, etc.), enzymes including but notlimited to protease, mannanase, cellulose, amylase, pectinase,xyloglucanase, natalase, termamyl, subtilisin, lactase, and any otheradjuvants may be included in appropriate, effective amounts. In someembodiments, such levels may be from about 0% to about 90%, or fromabout 0.001% to about 50%, or from about 0.01% to about 25% by weight.Alternatively, any given adjuvant or class of adjuvants may be presentat a level of from about 0.1 to about 10% by weight, or from about 0.1to about 5% by weight, or from about 0.1 to about 1% by weight.

Additional details of various adjuvants, their concentration amounts,and other details can be found in U.S. Pat. No. 8,287,755, hereinincorporated by reference.

III. Examples and Testing Results

As described above, the intercalated bleach compounds can be formed byevaporating water from an aqueous solution of calcium or sodiumhypochlorite solution mixed with magnesium salts such as magnesiumoxide. The intercalated bleach compounds have a molar ratio of alkalineearth metal to hypochlorite of greater than or equal to 3.

Various other alkali metal and alkaline earth metal salts may beincluded with the intercalated bleach compound in the intercalatedbleach composition. For example, alkaline earth oxides, alkaline earthhydroxides, alkaline earth carbonates, alkaline earth bicarbonates,alkaline earth chlorides, alkali chlorides, alkali carbonates, alkalibicarbonates, and combinations thereof may be mixed therewith. Specificexamples of such salts include, but are not limited to magnesium oxide,magnesium oxide adduct, magnesium hydroxide, magnesium hydroxide adduct,magnesium chloride trihydroxide, magnesium chloride pentahydroxide,magnesium carbonate, magnesium chloride, calcium oxide, calciumhydroxide, calcium carbonate, calcium chloride, sodium chloride, sodiumcarbonate, sodium bicarbonate, and combinations thereof. Hydrates ofsuch salts may also be included.

Magnesium oxide is a water insoluble, high isoelectric, inorganicmaterial. The high isoelectric point of magnesium oxide (e.g., about12-13) results in a solution/surface interface that is typicallypositively charged. The isoelectric point of a material is the pH atwhich the particular material carries no net electrical charge. Becausethe solution/surface interface is thus typically positively charged, themagnesium oxide has an affinity for interaction with anionic species. Itis believed that the positively charged magnesium oxide surface absorbsnegatively charged hypochlorite anions. Further reaction andintercalation of the hypochlorite anions with the magnesium oxide yieldsa previously unrecognized hypochlorite releasing material. Thisintercalated bleach compound is substantially different from thestarting materials, as evidenced by x-ray diffraction, yield ofreleasable hypochlorite, storage stability, solubility, and othercharacteristics.

Within the compositions prepared, the resulting product is a dry whitepowder, which is essentially odorless. When added to water, it resultsin a white suspension resembling milk of magnesia, with concurrentrelease of hypochlorite and a pH buffering range of about 8 to about11.5. The powder x-ray diffraction indicates a layered or intercalatedmaterial. Available chlorine can be tuned to values as low as about0.01% up to about 25%. More typical available chlorine values may befrom about 1% to about 25% or from about 2.5% to about 25%. The productcomposition may be a mixture of hydrated salts including, but notlimited to a magnesium hypochlorite adduct with a secondary magnesiumsalt, magnesium hydroxide, magnesium oxide, calcium carbonate, and/oradducts of one or more of the foregoing. The intercalated bleachcompound itself may be a hydrate. Such a hypochlorite releasing solidcan be used in any application where a solid hypochlorite is desired.

The buffering characteristics provided by the intercalated bleachcompound are at pH values (e.g., about 8 to about 11.5) generally moregentle than those typically associated with hypochlorite bleachcompositions, while providing excellent stability to the hypochloritespecies.

Advantageously, the method of manufacture does not use or produce anychlorine gas. Rather, the materials employed are readily available,economically priced, inorganic natural minerals. The intercalated bleachcompound itself may be considered to be derived from natural materials,not requiring use of any petrochemicals. Magnesium oxide is listed ashaving no limits in tolerance exemptions for active and inertingredients for use in antimicrobial formulations (e.g., food contactsurface sanitizing solutions) as detailed in 40 CFR 180-940. This mayexpand the potential disinfectant product applications that theintercalated bleach compound may be applied to, as compared to existinghypochlorite releasing products.

Various formulations of magnesium intercalated bleach were formed byproviding sodium hypochlorite solution or dissolving calciumhypochlorite solid (or lithium hypochlorite, or potassium hypochloritesolid) into water to make a solution including from about 10% to about18% of the alkali metal hypochlorite or alkaline earth metalhypochlorite. More generally, such a solution may include from about 3%to about 50%, or about 5% to about 25% of the hypochlorite salt. Where amixture of hypochlorite salts are included in the aqueous hypochloritesolution, the concentration ranges above may refer to the combinedconcentration of hypochlorite salts. Where employed, calciumhypochlorite can be mixed with water to solubilize the calciumhypochlorite and give the appropriate weight percent solution. Freshlymade calcium hypochlorite solution (e.g., as an intermediate fromchlorination of lime) may be used in place of solid calciumhypochlorite, and may be used as is, without addition of additionalwater, provided the concentration is within a desired range. Thehypochlorite solution may also be prepared by any process known in theliterature.

Where a hypochlorite is mixed with water, the reaction mixture may bestirred or otherwise mixed for an appropriate period of time (e.g.,about 2 to about 5 minutes). More generally, mixing may be from about0.5 minute to about 1 hour, or about 1 minute to about 10 minutes. Oncethe aqueous hypochlorite solution is provided, a magnesium or calciumsalt may be added thereto, in portions, while stirring (e.g., shearmixing) over an appropriate period of time (e.g., about 2 to about 10minutes, more generally 0.5 minute to about 1 hour or from 1 minute toabout 30 minutes). Once all the magnesium or calcium salt (e.g.,magnesium oxide) has been added, the reaction mixture may be mixed foran additional period of time of about 5 minutes to about 10 minutes, ormore generally from about 1 minute to about 24 hours, or about 2 minutesto about 6 hours or from about 5 minutes to 1 hour.

The reaction mixture may then be dried by pouring into an appropriatecontainer (e.g., a baking dish) and dried. The inventor formedintercalated bleach compound solids were dried for 16 to 72 hours attemperatures ranging from about 20° C. to about 80° C. More generally,drying time may be from about 1 hour to about 10 days, or from about 8hours to about 5 days. More generally, drying temperatures may rangefrom ambient temperature (e.g., about 20° C.) to about 200° C., or fromambient temperature to about 150° C. Temperatures above ambienttemperature may be achieved by drying in an oven. Once dried, the solidcan be broken up and powdered. Solid product may also be pressed or castinto a tablet, puck, or granule form. Of course, dried solid could alsobe used as is, without powdering granulating, or similar.

As will be appreciated, mixing or stirring mechanisms may be varied(e.g., with or without shear mixing), as may time of reaction, amount ofwater, concentration of hypochlorite solution, the ratio of hypochloritesalt to magnesium/calcium salt, exclusion or addition of carbon dioxide,drying methods (e.g., spray drying may be employed), and powderingmethod.

FIG. 1 plots available chlorine versus Mg to OCl ratios for severalmagnesium intercalated bleach compositions that were actually formed.Percentage yield versus Mg to OCl ratios are also plotted in FIG. 1. Forexample, as shown in FIG. 1, an intercalated bleach composition having aMg to OCl ratio of 3:1 had an available chlorine level of 25.5% and ayield of 83.7%. An intercalated bleach composition having a Mg to OClratio of 4:1 had an available chlorine level of 19.4% and a yield of88%. An intercalated bleach composition having a Mg to OCl ratio of5.9:1 had an available chlorine level of 18.1% and a yield of 99.6%. Anintercalated bleach composition having a Mg to OCl ratio of 13.9:1 hadan available chlorine level of 7.6% and a yield of 99%. An intercalatedbleach composition having a Mg to OCl ratio of 34.6:1 had an availablechlorine level of 3.7% and a yield of 91.9%.

As is apparent from FIG. 1, in an embodiment, as the Mg to OCl ratioincreases, the level of available chlorine generally decreases, whilethe percentage yield may generally increase.

FIG. 2A shows x-ray diffraction (“XRD”) angle data for an exemplarymagnesium intercalated bleach composition formed as described above.FIG. 2B shows comparative XRD data for dibasic magnesium hypochlorite(Mg(OCl)₂.2Mg(OH)₂). The data clearly show that the intercalated bleachcomposition has a XRD response that differs from that of dibasicmagnesium hypochlorite. The peak at 6.9 Å is indicative of a layered,intercalated structure (as is the 8.0 Å peak of the dibasic magnesiumhypochlorite, which is known to have a layered structure as well).

Mixtures of magnesium intercalated bleach (“MIB”) with 7.7% availablechlorine and solid form acids (e.g., potassium bisulfate, succinic acid,boric acid, etc.) were observed to exhibit complete stability (with nobleach loss) over a period of 6 weeks at ambient temperature. In otherwords, no significant acid-base reaction occurred, where the componentswere present in solid form, where water was substantially absent.

The shelf stability of exemplary magnesium intercalated bleach (“MIB”)was evaluated for compositions with and without a sodium lauryl sulfate(“SLS”) surfactant. Samples were tested by titration to determine theamount of hypochlorite remaining as compared to an initial amount. Fromthis measured difference, a shelf life was calculated, as shown in Table1 below.

TABLE 1 Initial Titration Final Titration Sample (wt % OCl) (wt % OCl)Difference Sample Age MIB 7.14 7.07 0.07 1.7 years MIB + SLS 7.55 7.210.34   3 years

Such extended shelf life stability characteristics (e.g., well over 1year, greater than 2 years, etc.) are among the best known amongchlorine bleach products.

In addition to the stability testing described above, the magnesiumintercalated bleach compositions were tested for their resistance tohumidity (i.e., their ability to resist degradation upon exposure tohumidity). The results were compared with the humidity stability ofalternative solid hypochlorite releasing products, specifically dibasicmagnesium hypochlorite and a mixture of calcium hypochlorite andmagnesium oxide. FIG. 3A shows humidity stability data after a period of2 months storage at a temperature of 80° F. and a relative humidity of80%. As shown, the initial weight percent hypochlorite was measured.Some samples were stored open, while others were stored closed, and theweight percentage of remaining hypochlorite was measured after the 2month storage.

As seen, the dibasic magnesium hypochlorite had an initial hypochloriteconcentration of about 25% by weight, with a reduction to nearly 0 forthe open sample after two months, and a reduction to about 22-23% byweight for the closed sample. The calcium hypochlorite/magnesium oxidemixture had an initial hypochlorite concentration of about 26% byweight, with a reduction to about 5% by weight for the open sample, anda reduction to about 22-23% by weight for the closed sample. The MIB hadan initial hypochlorite concentration of about 24% by weight, with areduction to about 18% by weight for the open sample, and a reduction toabout 23% by weight for the closed sample. The MIB exhibits much betterresistance to humidity than the other tested alternatives, particularlywhere the container is left open.

FIG. 3B shows humidity stability data after a period of 4.5 monthsstorage at a temperature of 80° F. and a relative humidity of 80%. Thecalcium hypochlorite/magnesium oxide mixture had an initial hypochloriteconcentration of about 4% by weight, with a reduction to about 1% byweight for the open sample, and a reduction to about 2.5% by weight forthe closed sample. Two MIB samples were tested. One MIB sample had aninitial hypochlorite concentration of about 5.5% by weight, with areduction to about 4.5% by weight for the open sample, and nostatistical significant reduction for the closed sample. The other MIBsample had an initial hypochlorite concentration of about 5.5% byweight, with no statistical significant reduction for either the closedor open samples.

The buffering characteristics of the MIB compositions, as well as theability to accelerate release of hypochlorite through addition of anacid were tested. It is believed that the MgO and/or Mg(OH)₂ componentpresent within the intercalated bleach compound acts to buffer the pH toa preferred region (e.g., about 8 to about 11.5) for enhancedhypochlorite stability. The results are shown in FIGS. 4A-4B. Acomparative example for dibasic magnesium hypochlorite is shown in FIGS.5A-5B. FIG. 4A plots the pH profile over time as hydrochloric acid (HCl)is added to the MIB aqueous solution at periodic intervals. The MIBcompound employed in FIGS. 4A-4B had a concentration of availablechlorine of 7.7% by weight (e.g., a Mg to OCl ratio of about 13.9:1 asshown in FIG. 1). The pH profile shows a relatively fast pH recovery,with buffering capability from about 8 to about 11.5.

FIG. 4B plots the concentration of hypochlorite in solution (ppm of OCl)as a function of how many millimoles of HCl are added. As seen, thehypochlorite release is generally linear until all of the hypochloritewithin the solid MIB is released (e.g., about 275-300 ppm OCl in FIG. 4Bafter addition of about 10 millimoles HCl).

FIGS. 5A-5B plot similar data as described above with respect to FIGS.4A-4B, but for a dibasic magnesium hypochlorite composition including34% available chlorine by weight. As seen in FIG. 5A, the bufferingrecovery is significantly slower and less complete than that exhibitedby the MIB compositions. In other words, this composition exhibitssignificantly lower buffering capacity. As such, the dibasic magnesiumhypochlorite is not capable of maintaining a relatively high pH for thesolution, as are the MIB compositions. Such improved buffering capacity(i.e., the ability to maintain a higher pH for longer) greatly improvesthe stability of the bleach composition. It is also observed that bleachrelease is not significantly aided by acid addition in the case ofdibasic magnesium hypochlorite, as higher bleach release than that shownin FIG. 5B is actually achieved with plain water.

Formulation stability and compatibility with various adjuvants, such asalcohol ethyoxylates (e.g., BIOSOFT N23-6.5), surfactants (e.g., sodiumlauryl sulfate, lauryl dimethyl amine oxide), polymers (e.g., SOKANLANCP 45 granules, ALCOSPERSE 747, propyl vinyl alcohol copolymer film, andquaternary ammonium compounds (e.g., benzyltrimethylammonium chloride,dodecyltrimethylammonium chloride) was tested. FIG. 6A showsdifferential scanning calorimetry (“DSC”) data which can be interpretedas comparative thermodynamic stability data for several different MIBcompositions including a wide range of concentrations of the alcoholethoxylate BIOSOFT N23-6.5. The results indicate that the MIBcompositions exhibit excellent compatibility and stability with a widevariety of adjuvants across a wide variety of concentrations.

By way of comparison, FIG. 6B shows less thermodynamic stability forsodium dichloroisocyanurate (“SDIC”) compositions with 10% of thealcohol ethoxylate BIOSOFT N23-6.5. The exothermic decompositionreaction of the SDIC and alcohol ethoxylate mixture (17 wt %hypochlorite and 10% alcohol ethoxylate; 240 J/g) is more than an orderof magnitude greater than the exothermic decomposition of the comparableMIB composition with alcohol ethoxylate (22 wt % hypochlorite and 7%alcohol ethoxylate; 16 J/g). In fact, even when the amount of alcoholethoxylate in the mixture with MIB has been more than doubled (18 wt %hypochlorite and 25% alcohol ethoxylate; 96 J/g), the SDIC mixture stillshows more than twice the exothermic energy release. Previously, suchisocyanurate salts have been regarded as having as good of formulaflexibility and compatibility as any chlorine bleach product available.In these cases, the invention MIB shows better formula flexibility andcompatibility than SDIC. Furthermore, such isocyanurate salts must beformulated with anhydrous materials, use of sodium hydroxide must beavoided (in fact basic conditions generally must be avoided), the saltscannot be formulated with hydroscopic materials, and the decompositionproducts of isocyanurate salts include NCl₃, which is particularlydangerous and undesirable. The MIB composition does not have theserestrictions.

FIG. 7A shows differential scanning calorimetry (“DSC”) data for anexemplary MIB composition, showing an endothermic decomposition reactionat about 375° C., requiring a substantial energy input of 420 J/g.Similar DSC data for calcium hypochlorite is shown in FIG. 7B, forcomparison. Calcium hypochlorite shows an exothermic decompositionreaction at about 212° C., giving off energy of 401 J/g, making calciumhypochlorite less desirable relative to the endothermic decompositionpathway of the present invention.

FIG. 7C shows DSC data for sodium dichloroisocyanurate, which includestwo endothermic reactions, one for loss of each water of hydration.While sodium dichloroisocyanurate exhibits no exothermic decompositionreactions in the temperature range of 10° C. to 200° C., it does formNCl₃ byproducts upon decomposition, which is dangerous and undesirable.

Because of the ability to carefully control release of hypochlorite withthe intercalated bleach compositions, active bleach can be delivered ondemand. For example, any suitable delivery mechanism may be employed,including, but not limited to, solid compositions (e.g., powders,granules, tablets, etc.), packets (e.g., pouches) including a solidcomposition, or aqueous liquids in which the intercalated bleach is insolution or suspension (e.g., an acid, or chelate, or surfactant, orfurther dissolution may be used to control hypochlorite concentrationand delivery).

Pouches may be formed from polyvinyl alcohol films or other sealablewater-soluble or dispersible polymer films. Solid product may be pressedor cast into a tablet, puck, or granule form where the solid solubilityis timed and bleach release may be slow and consistent over a givenperiod of time. The composition may be embedded or integrated into aplastic or polymer film, or may be attached to or embedded in asubstrate (e.g., polymer, plastic, nonwoven, other fabric, sponge,etc.).

Liquid compositions may be delivered through a trigger sprayer oraerosol delivery system. An embodiment may include a dual chamber bottleor package where two initially separate parts of the composition arecontacted with one another immediately prior to dispensing the product.For example, an acidic aqueous solution (e.g., including surfactant,chelating agents, dyes, fragrances, etc.) may be disposed in one chamberof the dual chamber bottle, and this liquid may be drawn through ormixed with the second part of the composition including the intercalatedbleach (e.g., a non-woven filtration system), so that the liquiddispensed includes hypochlorite bleach and the actives of the firstchamber (e.g., chelating agents, surfactants, dyes, fragrances, etc.).Of course, various adjuvants may be included within one or both parts ofsuch a two part composition, as desired.

By way of summary of the advantageous characteristics of theintercalated bleach compositions as compared to existing alternatives,Table 2 shows relative ratings for various criteria of several solidhypochlorite bleach products, where 5 represents “excellent”, 3represents “fair”, and 1 represents “poor”. As seen, the inventive MIBcompositions are the only products offering “excellent” formulaflexibility, low odor, and moisture tolerance. While some productsprovide better solution clarity or higher levels of available chlorine,the inventive intercalated bleach compounds and compositions provide byfar the best combination of high ratings from among the availablealternatives.

TABLE 2 Formula Minimal Solution Bleach Available Moisture Total ProductFlexibility Odor Clarity Stability Chlorine Tolerance Pts Intercalated 55 3 5 3 5 26 Bleach Ca(OCl)₂ 3 1 3 3 5 3 18 Li(OCl)₂ 1 1 5 1 3 3 14Na(OCl)₂ 3 3 5 1 1 3 16 phosphate adduct Isocyanuric acids 3 1 1 5 5 116 Isocyanurate salts 3 3 5 5 5 1 22 Dichlorohydantoin 1 3 1 5 5 1 16Trichloromelamine 1 1 1 5 5 3 16

The compositions described below are sample solid compositions ofM_(x)(OCl)_(y)(O)_(m)(OH)_(n).

Example 1

Example 1 illustrates a composition of the invention where the magnesiumsource is magnesium oxide and the bleach source is calcium hypochloritefor Mg_(13.9)Ca_(0.5)(OCl)O_(12.9)(OH).

In Example 1, we dissolve 79.5 grams of calcium hypochlorite (69.2 wt %)in 959.2 grams of water. Mix for 2 minutes. Add 430.5 grams of magnesiumoxide over 10 minutes with high shear mixing. Continue mixing for 10minutes after all magnesium oxide is added. Allow to dry in an opencontainer at room temperature. The product has 7.6% available chlorine.

Example 2

Example 2 illustrates a composition of the invention where the magnesiumsource is magnesium oxide, the bleach source is calcium hypochlorite andthe hypochlorite level is at a high percentage, forMg₃Ca_(0.5)(OCl)O₂(OH).

In Example 2, we dissolve 51.8 grams of calcium hypochlorite (69.2 wt %)in 186 grams of water. Mix for 2 minutes. Add 60.0 grams of magnesiumoxide over 10 minutes with high shear mixing. Continue mixing for 10minutes after all magnesium oxide is added. Allow to dry in an opencontainer at room temperature. The product has 25.5% available chlorine.

Example 3

Example 3 illustrates a composition of the invention where the magnesiumsource is magnesium oxide, the bleach source is calcium hypochlorite andthe hypochlorite level is at a low percentage, forMg_(34.6)Ca_(0.5)(OCl)O_(33.6)(OH).

In Example 3, we dissolve 8.9 grams of calcium hypochlorite (69.2 wt %)in 250.6 grams of water. Mix for 2 minutes. Add 120.2 grams of Magnesiumoxide over 5 minutes with high shear mixing. Continue mixing for 10minutes after all magnesium oxide is added. Allow to dry in an opencontainer. The product has 3.7% available chlorine.

Example 4

Example 4 illustrates a composition of the invention where the magnesiumsource is magnesium hydroxide, the bleach source is calcium hypochloriteand the hypochlorite level is at a high percentage, forMg₄Ca_(0.5)(OCl)(OH)₇.

In Example 4, we dissolve 18.35 grams of calcium hypochlorite (70.7 wt%) in 105.7 grams of water. Mix for 2 minutes. Add 42.8 grams ofmagnesium hydroxide over 5 minutes with high shear mixing. Continuemixing for 10 minutes after all magnesium hydroxide is added. Allow todry in an open glass container. The product has 6.4% available chlorine.

Example 5

Example 5 illustrates a composition of the invention where the magnesiumsource is magnesium hydroxide, the bleach source is calcium hypochloriteand the hypochlorite level is at a low percentage, forMg₃₃Ca_(0.5)(OCl)(OH)₆₅.

In Example 5, we dissolve 2.75 grams of calcium hypochlorite (57.5 wt %)in 98.7 grams of water. Mix for 2 minutes. Add 42.5 grams of magnesiumhydroxide over 5 minutes with high shear mixing. Continue mixing for 10minutes after all magnesium hydroxide is added. Allow to dry in an opencontainer. The product has 1.1% available chlorine.

Example 6

Example 6 illustrates a composition of the invention where the magnesiumsource is magnesium hydroxide, the bleach source is calcium hypochloriteand the hypochlorite level is at a mid-range percentage, forMg_(8.4)Ca_(0.5)(OCl)(OH)_(15.8).

In Example 6, we dissolve 17.8 grams of calcium hypochlorite (79 wt %)in 212.6 grams of water. Mix for 2 minutes. Add 95.8 grams of magnesiumhydroxide over 5 minutes with high shear mixing. Continue mixing for 10minutes after all magnesium hydroxide is added. Dry in an opencontainer. The product has 6.7% available chlorine.

Example 7

Example 7 illustrates a composition of the invention where the magnesiumsource is magnesium oxide, the bleach source is sodium hypochlorite andthe hypochlorite level is at a mid-range percentage, forMg_(11.9)(OCl)O_(10.9)(OH).

In Example 7, magnesium oxide (95.7 grams) was added to 234 grams ofsodium hypochlorite (6.4 wt % solution) over 5 minutes with high shearmixing. Continue mixing for 10 minutes after all magnesium oxide isadded. Dry in an open container at room temperature. The product has7.5% available chlorine.

Example 8

Example 8 illustrates a composition of the invention where the magnesiumsource is magnesium hydroxide, the bleach source is sodium hypochloriteand the hypochlorite level is at a mid-range percentage, forMg_(8.4)(OCl)(OH)_(15.8).

In Example 8, Magnesium hydroxide (95.8 grams) was added to 230 grams ofsodium hypochlorite (6.3 wt % solution) over 5 minutes with high shearmixing. Continue mixing for 10 minutes after all magnesium hydroxide isadded. Dry in an open container at room temperature. The product has2.7% available chlorine.

Without limitation, the following non-limiting examples illustrateimplementation of the present invention. Final formula is represented byM_(x)(OCl)_(y)(O)_(m)(OH)_(n), where M=Mg and Ca. For the purpose ofTables 3-8, Mg_(a)Ca_(b)(OCl)_(y)(O)_(m)(OH)_(n), where a+b=x.

TABLE 3 Reactant 1: Ca(OCl)₂ Reactant 2: MgO Product: PercentQuantitative Example Formula (grams) (grams) Available Chlorine Yield 9Mg₃Ca_(0.5)(OCl)(O)₂(OH) 51.8 60 25.5 83.7 10Mg_(4.5)Ca_(0.5)(OCl)(O)_(3.5)(OH) 51.7 91.3 19.4 88 11Mg_(5.9)Ca_(0.5)(OCl)(O)_(4.9)(OH) 51.9 120 18.2 99.6 12Mg_(13.9)Ca_(0.5)(OCl)(O)_(12.9)(OH) 79.5 430.5 7.6 99 13Mg_(34.6)Ca_(0.5)(OCl)(O)_(33.6)(OH) 8.9 120.2 3.7 91.9 14Mg_(50.8)Ca_(0.5)(OCl)(O)_(49.8)(OH) 2.6 43 1.7 75Based on final available chlorine levels for different samples, finalproducts are hydrates. Calcium salt impurities in starting calciumhypochlorite materials will be present in final product.

Without limitation, the following non-limiting examples illustrateimplementation of the present invention. Final formula is represented byM_(x)(OCl)_(y)(O)_(m)(OH)_(n), where M=Mg.

TABLE 4 Reactant 1: NaOCl Reactant 2: MgO Product: Percent QuantitativeExample Formula (grams) (grams) Available Chlorine Yield 15M_(3.1)(OCl)(O)_(2.1)(OH) 222.4 60.4 14.84 58.1 16M_(6.2)(OCl)(O)_(5.2)(OH) 222.3 120.3 9.98 60.2 17Mn_(11.9)(OCl)(O)_(10.9)(OH) 233.8 95.9 3.12 n/aBased on final available chlorine levels for different samples, finalproducts are hydrates. Sodium salts are present in final product.

Without limitation, the following non-limiting examples illustrateimplementation of the present invention. Final formula is represented byM_(x)(OCl)_(y)(OH)_(n), where M=Mg and Ca. For the purpose of Table Z,Mg_(a)Ca_(b)(OCl)_(y)(OH)_(n), where a+b=x.

TABLE 5 Reactant 1: Ca(OCl)₂ Reactant 2: Mg(OH)₂ Product: PercentQuantitative Example (grams) (grams) Available Chlorine Yield Formula 1818.4 42.77 6.43 47 Mg₄Ca_(0.5)(OCl)(OH)₇ 19 17.75 95.8 6.56 48Mg_(8.4)Ca_(0.5)(OCl)(OH)_(15.8) 20 15.33 127.3 6.15 n/aMg_(12.8)Ca_(0.5)(OCl)(OH)_(24.6) 21 2.75 42.5 1.19 47Mg₃₃Ca_(0.5)(OCl)(OH)₆₅ Footnote: Final products may be hydrates.Calcium salt impurities in starting calcium hypochlorite materials willbe present in final product.

Without limitation, the following non-limiting examples illustrateimplementation of the present invention.

TABLE 6 Example 22 Example 23 Example 24 Example 25 Example 26Ingredients Wt. % Wt. % Wt. % Wt. % Wt. %Mg_(12.8)Ca_(0.5)(OCl)(OH)_(24.6) 50 Mg_(8.4)Ca_(0.5)(OCl)(OH)_(15.8) 407 Mg₃Ca_(0.5)(OCl)(O)₂(OH) 10 Mg_(4.5)Ca_(0.5)(OCl)(O)_(3.5)(OH) 15sodium polyacrylate 1 alkyldiphenyloxide 3 disulfonate blue dye 0.1 0.01sodium xylene sulfonate 0.1 1 sodium lauryl sulfate 0.1 10% sulfuricacid 0.1 amine oxide 13 layered silicate 2 cetyldimethylbetaine 5 sodiumhydroxide (1N) 1 citric acid 45 sodium bicarbonate 35 sodium carbonate 5sodium chloride 5 cyclohexane 85 water 45.6 45 86

TABLE 7 Example 27 Example 28 Example 29 Example 30 Example 31Ingredients Wt. % Wt. % Wt. % Wt. % Wt. %Mg_(13.9)Ca_(0.5)(OCl)(O)_(12.9)(OH) 46 53 27 68 80 boric acid 54succinic acid 47 potassium bisulfate 73 benzyltrimethyl ammonium 32chloride dodecyltrimethyl 20 ammonium chloride

TABLE 8 Example 32 Example 33 Example 34 Example 35 Example 36Ingredients Wt. % Wt. % Wt. % Wt. % Wt. %Mg_(13.9)Ca_(0.5)(OCl)(O)_(12.9)(OH) 93 Mg₃Ca_(0.5)(OCl)(O)₂(OH) 93Mg_(12.8)Ca_(0.5)(OCl)(OH)_(24.6) 77 28 polyvinyl alcohol film 7 7dibasic calcium phosphate 23 alkylnapthalene sulfonate 3 Sodiumpolyacrylate 50 water 69

TABLE 9 Example 37 Example 38 Example 39 Example 40 Example 41Ingredients Wt. % Wt. % Wt. % Wt. % Wt. %Mg_(13.9)Ca_(0.5)(OCl)(O)_(12.9)(OH) 93.5 50 Mg₃Ca_(0.5)(OCl)(O)₂(OH) 9350 33 alcohol ethoxylate 6.5 50 7 50 Sodium polyacrylate 67

Without departing from the spirit and scope of this invention, one ofordinary skill can make various changes and modifications to theinvention to adapt it to various usages and conditions. As such, thesechanges and modifications are properly, equitably, and intended to be,within the full range of equivalence of the following claims.

The invention claimed is:
 1. A composition comprising: a bleach compoundhaving the formula:M_(x)(OCl)_(y)(O)_(m)(OH)_(n) wherein M is selected from the groupconsisting of magnesium, calcium and mixtures thereof; wherein x and yindependently equal any number greater than or equal to 1; wherein m andn independently equal any number greater than or equal to 0, but m and nare not both 0; and m+n≧7.
 2. The composition of claim 1, wherein M is acalcium.
 3. The composition of claim 1, further comprising a surfactant.4. The composition of claim 1, further comprising an acid.
 5. Thecomposition of claim 1, further comprising one or more alkaline earthmetal salts or alkali metal salts.
 6. The composition of claim 5,wherein alkali metal salts or alkaline earth metal salts are selectedfrom the group consisting of alkaline earth oxides, alkaline earthhydroxides, alkaline earth carbonates, alkaline earth bicarbonates,alkaline earth chlorides, alkali chlorides, alkali carbonates, alkalibicarbonates, and combinations thereof.
 7. The composition of claim 6,wherein alkali or alkaline earth salts are selected from the groupconsisting of magnesium oxide, magnesium hydroxide, magnesium chloridetrihydroxide, magnesium chloride pentahydroxide, magnesium carbonate,magnesium chloride, calcium oxide, calcium hydroxide, calcium carbonate,calcium chloride, sodium chloride, sodium carbonate, sodium bicarbonate,and combinations thereof.
 8. The composition of claim 1, wherein thebleach compound is a hydrate.
 9. The composition of claim 1, furthercomprising at least one member selected from the group consisting ofbuilders, surfactants, water soluble polymers, acids, fillers, diluents,desiccants, buffers, solid processing aids, preservatives, colorants,anti-corrosion inhibitors, dyes, fragrances, hydrotropes, polymerdispersants, chelating agents, water-swellable polymers, disinfectants,antimicrobials, essential oils, enzymes, and combinations thereof. 10.The composition of claim 1, wherein the composition is a solid.
 11. Thecomposition of claim 10, wherein the solid is in powder, granule, ortablet form.
 12. A composition comprising: a bleach compound having theformula:M_(x)(OCl)_(y)(O)_(m)(OH)_(n) wherein x and y independently equal anynumber greater than or equal to 1; wherein m and n independently equalany number greater than or equal to 0, but m and n are not both 0; andm+n≧7.
 13. The composition of claim 12, further comprising an acid. 14.The composition of claim 12, wherein the composition is a solid.
 15. Thecomposition of claim 12, further comprising one or more alkaline earthmetal salts or alkali metal salts.
 16. The composition of claim 15,wherein alkali metal salts or alkaline earth metal salts are selectedfrom the group consisting of alkaline earth oxides, alkaline earthhydroxides, alkaline earth carbonates, alkaline earth bicarbonates,alkaline earth chlorides, alkali chlorides, alkali carbonates, alkalibicarbonates, and combinations thereof.
 17. The composition of claim 16,wherein alkali or alkaline earth salts are selected from the groupconsisting of magnesium oxide, magnesium hydroxide, magnesium chloridetrihydroxide, magnesium chloride pentahydroxide, magnesium carbonate,magnesium chloride, calcium oxide, calcium hydroxide, calcium carbonate,calcium chloride, sodium chloride, sodium carbonate, sodium bicarbonate,and combinations thereof.
 18. The composition of claim 12, furthercomprising at least one member selected from the group consisting ofbuilders, surfactants, water soluble polymers, acids, fillers, diluents,desiccants, buffers, solid processing aids, preservatives, colorants,anti-corrosion inhibitors, dyes, fragrances, hydrotropes, polymerdispersants, chelating agents, water-swellable polymers, disinfectants,antimicrobials, essential oils, enzymes, and combinations thereof.
 19. Acomposition comprising: (a) a bleach compound having the formula:M_(x)(OCl)_(y)(O)_(m)(OH)_(n) wherein x and y independently equal anynumber greater than or equal to 1; wherein m and n independently equalany number greater than or equal to 0, but m and n are not both 0; andm+n≧7; and (b) a surfactant.